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OIC Intramedullary Nail System

FDA UDI

Class II (US FDA UDI)

by Orthopaedic Implant Company, The

Identity

Trade Name
OIC Intramedullary Nail System FDA UDI
Generic Name
Femur nail, non-sterile FDA UDI
Device Name
TROCHANTERIC FEMUR NAIL 11.5MM X 420MM RIGHT FDA UDI
Model / Reference
TAFN-115420R FDA UDI
Description
TROCHANTERIC FEMUR NAIL 11.5MM X 420MM RIGHT FDA UDI

Identifiers

Primary DI / UDI-DI
10811998037919 FDA UDI
510(k) Number
K150655 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Femur nail, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 11.5 Millimeter FDA UDI
Length — 420 Millimeter FDA UDI

Category: Femur nail, non-sterile

OIC Intramedullary Nail System by Orthopaedic Implant Company, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femur nail, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1e863d50-855b-4963-9289-a145c2849d85 36 fields · synced May 30, 2026